美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA090162"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
50090-2203-3 50090-2203 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20240202 N/A ANDA ANDA090162 A-S Medication Solutions TOPIRAMATE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (50090-2203-3)
71205-187-30 71205-187 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA090162 Proficient Rx LP TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-187-30)
71205-187-60 71205-187 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA090162 Proficient Rx LP TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-187-60)
71205-187-90 71205-187 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA090162 Proficient Rx LP TOPIRAMATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-187-90)
71205-202-90 71205-202 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA090162 Proficient Rx LP TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-202-90)
29300-118-01 29300-118 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20130701 N/A ANDA ANDA090162 Unichem Pharmaceuticals (USA), Inc. TOPIRAMATE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-118-01)
29300-118-05 29300-118 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20130701 N/A ANDA ANDA090162 Unichem Pharmaceuticals (USA), Inc. TOPIRAMATE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-118-05)
29300-118-10 29300-118 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20130701 N/A ANDA ANDA090162 Unichem Pharmaceuticals (USA), Inc. TOPIRAMATE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-118-10)
29300-118-16 29300-118 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20130701 N/A ANDA ANDA090162 Unichem Pharmaceuticals (USA), Inc. TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-118-16)
68071-4760-3 68071-4760 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190208 N/A ANDA ANDA090162 NuCare Pharmaceuticals,Inc. TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4760-3)
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